Friday, May 19, 2023

‘Electrifying’ achievement for making more sustainable polymers

New low-cost material can be made with minimal power and no hazardous chemicals

Peer-Reviewed Publication

FLINDERS UNIVERSITY

chemical reaction 

IMAGE: FLINDERS UNIVERSITY CHEMISTS HAVE DISCOVERED A NEW WAY TO MAKE ‘GREEN’ POLYMERS FROM LOW-COST BUILDING BLOCKS WITH JUST A SMALL AMOUNT OF ELECTRICITY. view more 

CREDIT: FLINDERS UNIVERSITY

Chemistry researchers at Flinders University have ‘struck gold’ by discovering a new way to make ‘green’ polymers from low-cost building blocks with just a small amount of electricity.

The reaction is fast and occurs at room temperature. No hazardous chemical initiators are required – just electricity, with many potential uses including in gold mining and recycling e-waste, an interdisciplinary team reveal in an article just published in the prestigious Journal of the American Chemical Society

While hundreds of millions of tonnes of plastic is produced every year, with up to half used for single purposes, the Flinders University research group is working on more sustainable options. The power used in production is a contributor to pollution and global warming.

“The use of electricity to produce new materials is an emerging field of research that opens many doors to new chemicals and polymers that can be produced in a more sustainable way,” says co-author Dr Thomas Nicholls, an expert in using electrochemistry to make valuable molecules. 

The process begins by adding an electron to the basic building block or monomer. After ‘electrocuting’ the monomer, it reacts with another building block in a chain reaction which leads to the formation of a polymer.

First-author and PhD candidate Jasmine Pople says: “Our method to electrochemically produce polymers provides new materials that are highly functional and environmentally friendly.”

“The use of electricity to make valuable molecules is expanding rapidly due to its versatility. Additionally, it may generate less waste than traditional chemical syntheses and it can be powered with renewable energy.”

The key polymer made by the team has sulfur-sulfur bonds in its backbone. These sulfur groups can do useful things like bind precious metals such as gold. The team demonstrated that the key polymer could remove 97% of gold from solutions of relevance to mining and e-waste recycling.

The sulfur-sulfur bonds can also be broken and reformed. This interesting property enabled the team to discover conditions to convert the polymer back to its original building block. This is an important advance in recycling.

Typically, when common plastics are recycled, they are simply heated and reshaped into a new product. This process can cause degradation and down-cycling (conversion to a less valuable material), leading to eventual disposal in landfill.

In contrast, the polymers made in the latest research from Flinders University scientists can be chemically converted back into its constituent building blocks in high yield – meaning that building block can be used again to make new polymers.

The team also carried out quantum mechanical calculations to understand the details of how the reaction works. The findings were surprising and fortuitous.

“The polymerisation has a clever self-correcting mechanism: whenever the wrong reaction occurs, it reverses until the correct reaction proceeds, ensuring a uniform polymer,” says Research Associate in computational and physical chemistry Dr Le Nhan Pham

Future applications of this class of materials include environmental remediation, gold mining, and use of the polymer as an anti-microbial agent.

This work is funded by an ARC Discovery grant ‘Unusual Trisulfide Chemistry’, led by Future Fellow and Matthew Flinders Professor of Chemistry Justin Chalker and Associate Professor Zhongfan Jia in collaboration with Dr Tom Hasell at the University of Liverpool (DP230100587).

The paper ‘Electrochemical synthesis of poly(trisulfides)’ has been published in the Journal of the American Chemical Society (JACS) DOI: 10.1021/jacs.3c03239

https://pubs.acs.org/doi/full/10.1021/jacs.3c03239#

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